US6542769B2ExpiredUtilityPatentIndex 83
Imaging system for obtaining quantative perfusion indices
Est. expiryDec 18, 2020(expired)· nominal 20-yr term from priority
A61B 5/0263A61B 5/4064A61B 5/0275
83
PatentIndex Score
42
Cited by
29
References
17
Claims
Abstract
A bolus containing optical and MRI contrast agents is administered to a patient for determining quantitative perfusion indices from perfusion weighted magnetic resonance imaging analysis (PWI). The optical contrast agent time-concentration data, which can be obtained non-invasively, is used to define an arterial input function. The MRI contrast agent time concentration can be non-invasively determined using MRI to define a tissue function. An MRI time-signal curve can be determined by deconvolving the arterial and tissue functions. In one embodiment, SVD is used to determine a residue function from which a flow map can be computed.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1. A method for determining quantitative blood perfusion indices, comprising:
administering a bolus containing an optical contrast agent and an MRI (Magnetic Resonance Imaging) contrast agent;
determining an arterial input function from optical contrast agent concentration samples after the bolus was administered;
determining a tissue function from MRI contrast agent samples in a tissue volume of interest, wherein the contrast optical agent concentration samples and the MRI contrast agent concentration samples are correlated in time;
determining at least one quantitative perfusion index from the arterial input function and the tissue function.
2. The method according to claim 1 , wherein the optical contrast agent includes ICG (Indocyanine Green).
3. The method according to claim 1 , wherein the MRI contrast agent includes Gd-DTPA (Gadopentetate dimeglumine pentaacetic acid).
4. The method according to claim 1 , further including deconvolving an MR signal-time curve from the arterial input function and the tissue function to derive the at least one quantitative perfusion index.
5. The method according to claim 4 , further including using SVD (Singular Value Decomposition) to deconvolve the MR signal time curve.
6. The method according to claim 4 , further including computing a flow map or a blood volume map.
7. The method according to claim 6 , further including determining a residue function from the arterial input function and the tissue function and using the residue function to compute the flow map.
8. The method according to claim 1 , further including using optical densitometry to determine the optical contrast agent concentration.
9. The method according to claim 1 , further including taking blood samples to determine the optical contrast agent concentration.
10. A method for determining quantitative perfusion indices, comprising:
administering a bolus containing an optical contrast agent and an MRI (Magnetic Resonance Imaging) contrast agent;
determining an arterial input function C a (t) from the optical contrast agent;
determining a tissue function C VOI (t) from the MRI contrast agent;
deconvolving an MR signal-time curve from the arterial input function C a (t) and the tissue function C VOI (t) based on C VOI ( t ) = F t ∫ 0 t C a ( τ ) R ( t - τ ) τ ,
where R(t) is a residue function describing the fraction of MRI contrast agent at time t, and F t represents tissue flow.
11. The method according to claim 10 , further including using SVD (Singular Value Decomposition) to deconvolve the MR signal-time curve.
12. The method according to claim 10 , wherein the optical contrast agent includes ICG (Indocyanine Green) and the MRI contrast agent includes GDA (gadopentate dimefluminepentaacetic acid).
13. The method according to claim 10 , wherein the bolus comprises about 0.125 mg/ml ICG (Indocyanine Green) and about 457 mg mg/ml GDA (gadopentate dimefluminepentaacetic acid).
14. A bolus solution for intravascular injections comprising:
an optical contrast agent including Idocyanine Green; and
an MRI (Magnetic Resonance Imaging) contrast agent including gadopentate dimegluminepentaacetic acid.
15. The solution according to claim 14 , wherein the Indocyanine Green has a concentration ranging from about 0.01 to 50% by weight based on the total weight of the composition.
16. The solution according to claim 14 , wherein the gadopentate dimegluminepentaacetic acid has a concentration ranging from about 0.001M to about 0.5M.
17. The solution according to claim 14 , wherein the optical contrast agent can provide an arterial input function and the MRI (Magnetic Resonance Imaging) contrast agent can provide a tissue function.Cited by (0)
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